Variant report

Variant rs537880655
Chromosome Location chr4:20447082-20447083
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:20444000-20449000 Enhancers Colon Smooth Muscle Colon
2 chr4:20444200-20449600 Enhancers Fetal Lung lung
3 chr4:20444800-20447600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr4:20445600-20447400 Weak transcription Fetal Kidney kidney
5 chr4:20446200-20447400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr4:20446200-20449200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr4:20446600-20447400 Weak transcription Fetal Stomach stomach
8 chr4:20446600-20447800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr4:20446600-20447800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr4:20446600-20448200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr4:20446800-20447200 Weak transcription Rectal Smooth Muscle rectum
12 chr4:20446800-20447800 Weak transcription Placenta Amnion Placenta Amnion
13 chr4:20447000-20448800 Enhancers NHDF-Ad bronchial

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